ACCURATE DETECTION OF RARE GENETIC VARIANTS IN NEXT GENERATION SEQUENCING

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United States of America Patent

APP PUB NO 20170016056A1
SERIAL NO

15124286

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ATTORNEY / AGENT: (SPONSORED)

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Abstract

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The invention relates to a method for analyzing a target nucleic acid fragment, comprising generating a first strand using one strand of the target as a template by primer extension, using a first oligonucleotide primer which comprises, from 5′ to 3′, an overhang adaptor region, a primer ID region and a target specific sequence region complementary to one end of the target fragment; optionally removing non-incorporated primers; amplifying the target from the generated first strand to produce an amplification product; and detecting the amplification product. Also disclosed are unique primers useful for such target analysis methods.

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Patent Owner(s)

Patent OwnerAddress
CLARIENT DIAGNOSTIC SERVICES INC31 COLUMBIA AVENUE ALISO VIEJO CA 92656

International Classification(s)

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  • 2015 Application Filing Year
  • C12Q Class
  • 3483 Applications Filed
  • 2244 Patents Issued To-Date
  • 64.43 % Issued To-Date
Click to zoom InYear of Issuance% of Matters IssuedCumulative IssuancesYearly Issuances201520162017201820192020202120222023202420250255075100

Inventor(s)

Inventor Name Address # of filed Patents Total Citations
Nelson, John Richard Niskayuna, US 82 579
Szkotnicki, Lee Thomas Houston, US 1 9
Tan, Xin-Xing Houston, US 1 9
Thomas, Kenneth Bradford Houston, US 1 9

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Patent Citation Ranking

  • 9 Citation Count
  • C12Q Class
  • 52.11 % this patent is cited more than
  • 8 Age
Citation count rangeNumber of patents cited in rangeNumber of patents cited in various citation count ranges2682212021779161049531101 - 1011 - 2021 - 3031 - 4041 - 5051 - 6061 - 7071 - 8081 - 9091 - 100100 +020040060080010001200140016001800200022002400260028003000

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